A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039473



Internal ID94034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101432143..101672707hg38UCSC Ensembl
chr10:103191900..103432464hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38240565
hg19240565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474831
Supporting Variants
Samples
Known GenesBTRC, DPCD, FBXW4, MIR3158-1, MIR3158-2, POLL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039473
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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